1
2
3
4
5
6
and
atrophy
autosomal
a
b
c
d
blood
cell
combined
congenital
defect
deficiency
dependent
disease
disorder
dominant
due
dysplasia
familial
group
hereditary
i
ii
iii
infantile
isolated
juvenile
linked
marie
mental
multiple
muscular
neonatal
of
onset
primary
progressive
recessive
related
resistance
retardation
susceptibility
syndrome
to
tooth
type
with
x